A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15759355



Internal ID2552386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80631174..80640232hg38UCSC Ensembl
chr17:78604974..78614032hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg389059
hg199059
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641381
Supporting Variants
SamplesHG02266
Known GenesRPTOR
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15759355
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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